Targeted metabolomics reveals plasma short-chain fatty acids are associated with metabolic dysfunction-associated steatotic liver disease

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  • Mira Thing
  • Mikkel Parsberg Werge
  • Nina Kimer
  • Liv Eline Hetland
  • Elias Badal Rashu
  • Puria Nabilou
  • Anders Ellekaer Junker
  • Elisabeth Douglas Galsgaard
  • Bendtsen, Flemming
  • Johnny Laupsa-Borge
  • Adrian McCann
  • Gluud, Lise Lotte
Background
Alterations in the production of short-chain fatty acids (SCFAs) may reflect disturbances in the gut microbiota and have been linked to metabolic dysfunction-associated steatotic liver disease (MASLD). We assessed plasma SCFAs in patients with MASLD and healthy controls.

Methods
Fasting venous blood samples were collected and eight SCFAs were measured using gas chromatography-tandem mass spectrometry (GC-MS/MS). Relative between-group differences in circulating SCFA concentrations were estimated by linear regression, and the relation between SCFA concentrations, MASLD, and fibrosis severity was investigated using logistic regression.

Results
The study includes 100 patients with MASLD (51% with mild/no fibrosis and 49% with significant fibrosis) and 50 healthy controls. Compared with healthy controls, MASLD patients had higher plasma concentrations of propionate (21.8%, 95% CI 3.33 to 43.6, p = 0.02), formate (21.9%, 95% CI 6.99 to 38.9, p = 0.003), valerate (35.7%, 95% CI 4.53 to 76.2, p = 0.02), and α-methylbutyrate (16.2%, 95% CI 3.66 to 30.3, p = 0.01) but lower plasma acetate concentrations (− 30.0%, 95% CI − 40.4 to − 17.9, p < 0.001). Among patients with MASLD, significant fibrosis was positively associated with propionate (p = 0.02), butyrate (p = 0.03), valerate (p = 0.03), and α-methylbutyrate (p = 0.02). Six of eight SCFAs were significantly increased in F4 fibrosis.

Conclusions
In the present study, SCFAs were associated with MASLD and fibrosis severity, but further research is needed to elucidate the potential mechanisms underlying our observations and to assess the possible benefit of therapies modulating gut microbiota.
OriginalsprogEngelsk
Artikelnummer43
TidsskriftBMC Gastroenterology
Vol/bind24
Udgave nummer1
Antal sider10
ISSN1471-230X
DOI
StatusUdgivet - 2024

Bibliografisk note

Funding Information:
The targeted metabolomics were performed at Bevital AS ( https://bevital.no/ ). The study was financially supported by Novo Nordisk and grants from The Danish Medical Associations Research Fund.

Funding Information:
Open access funding provided by Copenhagen University. This work was financially supported by Novo Nordisk and grants from The Danish Medical Associations Research Fund. (Grant number 2021-0085). Author Lise Lotte Gluud has received research support from Alexion, Gilead Sciences and Novo Nordisk.

Publisher Copyright:
© 2024, The Author(s).

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